chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171531557215315573TC24GENIChomozygous110967504
171531582815315829CT28GENIChomozygous110967506
171531599015315991GC20GENIChomozygous110967508
171531613015316131GC29GENIChomozygous111171533
171531675015316751AG21GENIChomozygous111171535
171531764715317648TA11GENIChomozygous110967514
171531879515318796GT31GENIChomozygous110967516
171532116115321162TC28GENIChomozygous111171537
171532131815321319AG23GENIChomozygous111171539
171532136015321361AC24GENIChomozygous111171541
171532205815322059GA21GENIChomozygous111171545
171532244015322441TC18GENIChomozygous111171547
171532245915322460AT21GENIChomozygous111171549
171532252715322528GA27GENIChomozygous111171551
171532271615322717GT16GENIChomozygous110967520
171532310915323110TG23GENIChomozygous110967522
171532344015323441AC12GENIChomozygous110967524
171533016115330162TC26GENIChomozygous110967530
171533021915330220CA23GENICpossibly homozygous110967532
171533061215330613CG22GENIChomozygous110967534
171533076515330766AC20GENIChomozygous110967536
171533117015331171AG19GENIChomozygous110967538
171533128515331286GC14GENIChomozygous110967540
171533237115332372AG35GENIChomozygous111171554
171533260315332604TC36GENIChomozygous110967542
171533267415332675GC33GENIChomozygous110967544
171533310215333103TG26GENIChomozygous110967546
171533321115333212CT27GENIChomozygous110967548
171533406115334062CT24GENIChomozygous110967550
171533459615334597TC22GENIChomozygous110967552
171533480815334809CA25GENIChomozygous110967554
171533531815335319CT33GENIChomozygous111171556
171533740515337406AG40GENIChomozygous110967560
171533876615338767TA19GENIChomozygous110967562
171533884615338847TA18GENIChomozygous110967564
171532985115329852CT20GENIChomozygous111231702
171531967215319673GA18GENIChomozygous111231700